Cardiopulmonary Resuscitation Aid Kit
The Cardiopulmonary Resuscitation Aid Kit (product code OEV) is an anesthesiology convenience kit containing devices used to support cardiopulmonary resuscitation (CPR) efforts. Established under the May 1997 FDA Convenience Kits Interim Regulatory Guidance, it is under enforcement discretion and does not require a 510(k) submission provided all guidance criteria are satisfied. This device is FDA Class 2 under regulation 868.5915 in the Anesthesiology specialty. It carries no implant or life-sustaining flags.
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Basic Information
- Product Code
- OEV
- Device Class
- FDA class 2
- Regulation Number
- 868.5915
- Medical Specialty
- Anesthesiology
- Review Panel
- AN
- Submission Type
- 7
Device Characteristics
Definition
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
FEI Numbers
This FDA classification entry is associated with 19 FEI numbers. Click on an entry to view related FDA registrations.
Registration Numbers
This FDA classification entry is associated with 19 registration numbers. Click on an entry to view related FDA registrations.